@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_head {
  this: np:hasAssertion dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_assertion;
    np:hasProvenance dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_provenance;
    np:hasPublicationInfo dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_assertion a np:Assertion .
  
  dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_provenance a np:Provenance .
  
  dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_assertion {
  miriam-gene:657 a ncit:C16612 .
  
  lld:C0032584 a ncit:C7057 .
  
  dgn-gda:DGN40ebe3c8fc4106362326899c8b78d620 sio:SIO_000628 miriam-gene:657, lld:C0032584;
    a sio:SIO_001121 .
}

dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_provenance {
  dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_assertion dcterms:description
      "[If patients present with mixed morphology polyps in the large bowel that are autosomal dominantly inherited and corresponding absence of upper gastrointestinal abnormalities, the gene to begin mutation screening should be BMPR1A rather than APC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:19773747;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:31+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}